Complexity of PEDF multifunctional signaling in retinal development and diseases

retinas, and define receptor-specific signaling using siRNA and pharmacological inhibition. These receptors are broadly expressed in retinoblasts and acquire cell-type-specific patterns during retinal maturation via PEDF-independent mechanisms. LR and LRP6 also colocalize at the outer limiting membrane (OLM). Functionally, PEDF activates AKT, STAT3, ERK, and p38 and suppresses β-catenin in both HUVEC and ARPE-19 cells, while mTOR activation remains receptor-independent. LR and LRP6 couple PEDF to STAT3 and β-catenin in HUVECs, whereas in ARPE-19 cells LR links PEDF to AKT/STAT3/ERK and LRP6 to AKT/β-catenin. ATGL inhibition abolishes PEDF-induced AKT/STAT3/ERK/p38 signaling in both cell types. A 17-mer PEDF mimetic (Ppx) recapitulates these effects. These findings help define a framework for PEDF pleiotropy and highlight the OLM as a therapeutic interface.

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Publication Details

Journal
Communications Biology
Published
2026-05-08
DOI
https://doi.org/10.1038/s42003-026-10175-2
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Complexity of PEDF multifunctional signaling in retinal development and diseases

Colin J. Barnstable, Joyce Tombran‐Tink, Xiaomin Zhang, Mingliang Zhang et al.
Communications Biology
Retinal Development and Disorders
article

Complexity of PEDF multifunctional signaling in retinal development and diseases

Colin J. Barnstable, Joyce Tombran‐Tink, Xiaomin Zhang, Mingliang Zhang, Xiaorong Li, Changjie Ren, Zihao Yu
article en

Abstract

retinas, and define receptor-specific signaling using siRNA and pharmacological inhibition. These receptors are broadly expressed in retinoblasts and acquire cell-type-specific patterns during retinal maturation via PEDF-independent mechanisms. LR and LRP6 also colocalize at the outer limiting membrane (OLM). Functionally, PEDF activates AKT, STAT3, ERK, and p38 and suppresses β-catenin in both HUVEC and ARPE-19 cells, while mTOR activation remains receptor-independent. LR and LRP6 couple PEDF to STAT3 and β-catenin in HUVECs, whereas in ARPE-19 cells LR links PEDF to AKT/STAT3/ERK and LRP6 to AKT/β-catenin. ATGL inhibition abolishes PEDF-induced AKT/STAT3/ERK/p38 signaling in both cell types. A 17-mer PEDF mimetic (Ppx) recapitulates these effects. These findings help define a framework for PEDF pleiotropy and highlight the OLM as a therapeutic interface.

Communications Biology
Harrisburg University of Science and Technology (US), Tianjin Medical University Eye Hospital (CN), Tianjin Medical University (CN), Penn State Milton S. Hershey Medical Center (US)
National Natural Science Foundation of China, Natural Science Foundation of Tianjin City
Openalex Percentile: Top 8%
Retinal Development and Disorders
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